Anchoring system for use with neonates

ABSTRACT

A catheter securement device holds a medical article by securing an anchor member to an attachment region of a neonate. The attachment region is located on the body of the neonate. The catheter securement device defines a central channel into which at least a portion of the medical article is inserted. The catheter securement device includes at least one mounting wing and a body member. The mounting wing contacts the anchor member over the attachment region and lifts the medical article away from the neonate&#39;s skin. At least a portion of the body member is located in a distal direction from the attachment region and does not directly contact the neonate&#39;s skin. A soft material may be inserted between the distal portion of the body member and the neonate&#39;s skin to further inhibit rocking of the medical article upon the neonate.

RELATED APPLICATIONS

This application claims priority under 35 U.S.C. §119(e) to U.S.Provisional Patent Application Ser. No. 60/685,182, filed May 26, 2005,and which is hereby expressly incorporated by reference in its entirety.

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to a securement system used to attach a medicalline to a premature baby's or neonate's skin.

2. Description of the Related Art

It is common in the treatment of patients for healthcare providers toutilize catheters to introduce fluids and medications directly into thepatient or to withdraw fluids from the patient. Premature babies usuallyrequire assistance to breathe and eat, and thus, are often fullyinstrumented. These babies also are usually fed intravenously by anintravenous (IV) catheter inserted into a vein, usually on the dorsalside of the neonate's hand or forearm. An arterial catheter may also beinserted on the ventral side of the neonate's hand for purposes ofmonitoring blood oxygenation.

Premature babies'present additional challenges to healthcare personnelsince premature babies have less skin surface area available forattachment of a catheter. For premature babies, each catheter isprecisely positioned, and the position of such is fixed relative to theneonate to prevent migration or dislodgment. Healthcare personnelusually secure the (IV) and arterial catheters using tape (and sometimesusing sutures). The catheters remain in place for several days or weeks,and often require repositioning and/or replacement on a periodic basis.

Securing a catheter with tape upon the patient traditionally has certaindrawbacks. The use of tape at the insertion site can retain dirt orother contaminant particles, potentially leading to infection of theneonate. Tape also fails to limit catheter motion and, therefore,contributes to motion related complications like phlebitis, infiltrationand catheter migration.

Taped dressings also require periodic changes. The frequent, oftendaily, removal and reapplication of adhesive tape to the skin of thepatient can exfoliate the upper layers of the neonate's skin in the areaaround the dressing. Such exfoliation of the upper layers of skin canlead to abrasions on the neonate's skin because the neonate's skin is sothin, sensitive and fragile. Moreover, infection and disease can occuras a result of such skin wounds owing to the relatively undevelopednature of a neonate's immune system.

Such repeated applications of tape over the catheter or medical line canadditionally lead to the build up of adhesive residue on the outersurface of the catheter or medical line. This residue can result incontaminants adhering to the catheter itself, increasing the likelihoodof infection of the insertion site. This residue can also make thecatheter or medical line stickier and more difficult to handle forhealthcare providers.

Catheter systems have been developed for neonate applications. Eventhough the limited skin surface area of a premature baby may warrant theuse of a reduced or miniature sized catheter, the use of such smallcatheters would import additional difficulties for healthcare personnelduring the treatment of the premature baby. Thus, catheter manufacturersoften size their catheters to facilitate handling and manipulation byhealthcare personnel.

The attachment region on a catheter retention device may be larger thanthe available skin surface of a neonate. Further, when the tip of thecatheter is aligned with the insertion site on a neonate, the body ofthe catheter may extend beyond the available skin surface. Due to therelative size difference between the available skin surface of a neonateand the length of the catheter, these systems tend to be relativelylarge and may result in the skin attachment location of the catheterretention device being located at an undesirable distance from theinsertion site.

SUMMARY OF THE INVENTION

The systems and methods of the present invention have several features,no single one of which is solely responsible for its desirableattributes. Without limiting the scope of this invention as expressed bythe claims which follow, its more prominent features will now bediscussed briefly. After considering this discussion, and particularlyafter reading the section entitled “Detailed Description of thePreferred Embodiments,” one will understand how the features of thisinvention provide several advantages over traditional cathetersecurement techniques.

An aspect of the present invention involves a securement device foranchoring a medical article to a patient's skin. The securement devicecomprises at least one anchor member that has a lower adhesive surfaceconfigured to attach to skin of a patient and a retainer. The retainercomprises a body member that has a channel formed therethrough about achannel axis and that terminates at a proximal end of the body member.The channel retains at least a portion of the medical article and has alongitudinal access opening to allow at least ingress of the portion ofthe medical article into the channel. The retainer further comprises atleast one abutment that extends generally normal to the channel axis soas to inhibit longitudinal movement of the retained portion of themedical article relative to the body member. The retainer furthercomprises at least one mounting wing that supports the body member andhas an attachment portion mounted on the anchor member. The attachmentportion is disposed entirely to one side of and beyond the proximal endof the body member.

Another aspect of the present invention involves a securement device foranchoring a medical article to a patient's skin. The securement devicecomprises one or more anchor members having a lower adhesive surfaceconfigured to attach to skin of a patient and a retainer. The retainercomprises a body member that has a channel formed therethrough about achannel axis. The channel retains at least a portion of the medicalarticle and has a longitudinal access opening to allow at least ingressof the portion of the medical article into the channel. The retainerfurther comprises at least one abutment that extends generally normal tothe channel axis so as to inhibit longitudinal movement of the retainedportion of the medical article relative to the body member. The retainerfurther comprises at least a pair of mounting wings that support thebody member. Each mounting wing has an attachment portion mounted on theone or more anchor members. The attachment portions are spaced apartfrom each other to define an insertion side space. The mounting wingstogether support the body member at a position distal of the insertionside space.

An additional aspect of the present invention involves a securementdevice for anchoring a medical article to a patient's skin. Thesecurement device comprises at least one anchor member that has a loweradhesive surface configured to attach to skin of a patient and aretainer. The retainer comprises a body member that has a channel formedtherethrough about a channel axis. The channel retains at least aportion of the medical article and has a longitudinal access opening toallow at least ingress of the portion of the medical article into thechannel. The channel has a longitudinal midpoint. The retainer furthercomprises at least one support disposed to a side of the channel axisand that has an attachment portion mounted on the anchor member. Theattachment portion has a longitudinal midpoint that is offset from thelongitudinal midpoint of the channel along a longitudinal axis.

Another aspect of the present invention involves a securement device foranchoring a medical article to a patient's skin. The securement devicecomprises at least one anchor member that has a lower adhesive surfaceconfigured to attach to skin of a patient and a retainer. The retainercomprises a body member that has a channel formed therethrough about achannel axis. The channel retains at least a portion of the medicalarticle and has a longitudinal access opening to allow at least ingressof the portion of the medical article into the channel. The channel hasa longitudinal midpoint. The retainer further comprises at least onesupport that is mounted on the anchor member. The body member iscantilevered from the support so as to suspend the body member off thebody of the patient.

Another aspect of the present invention involves a securement device foranchoring a medical article to a patient's skin. The securement devicecomprises an anchor member and a retainer. The retainer comprises a bodymember that includes a channel formed therethrough. The channel retainsa portion of the medical article and has a longitudinal access openingdisposed on an underside of the body member to allow ingress of themedical article into the channel. The retainer further comprises atleast one abutment that extends generally normal to an axis of thechannel to inhibit longitudinal movement of the medical article. Theretainer further comprises at least one mounting wing that supports thebody and has an attachment portion mounted to the anchor member. Anoverall longitudinal length of the at least one mounting wing exceedsthe longitudinal length of the attachment portion.

Another aspect of the present invention involves a method of securing amedical article to a skin surface of a patient. The method comprisesproviding a medical article, selecting an attachment region on thesurface of the patient for inserting the medical article, and providinga retainer having a channel formed therethrough and at least oneabutment. The channel is disposed to a distal side of the retainer toreceive and retain the medical article. The at least one abutmentextends generally normal to the channel. The method further comprisespositioning the retainer on the medical article, pressing the medicalarticle into the channel through an opening formed on the underside ofthe retainer, and abutting the medical article against the abutment toinhibit longitudinal motion of the medical article relative to theretainer in at least one direction. The method further comprisesaligning an attachment portion of the retainer with the attachmentregion on the patient so that a substantial portion of the channel islocated outside of the attachment region and adhering the retainer to atleast the attachment region on the patient.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other features, aspects, and advantages of the presentinvention will now be described in connection with preferred embodimentsof the invention, in reference to the accompanying drawings. Theillustrated embodiments, however, are merely examples and are notintended to limit the invention.

FIG. 1 is a perspective view of a securement device that is configuredin accordance with a preferred embodiment of the present invention.

FIG. 2 is a top plan view of the securement device of FIG. 1 whichincludes a retainer and first and second anchor members.

FIG. 3 is a top plan view of the first anchor member of FIG. 2.

FIG. 4 is a top plan view of the second anchor member of FIG. 2.

FIG. 5 is a top plan view of the retainer of FIG. 2.

FIG. 6 is a front side view of the retainer of FIG. 5.

FIG. 7 is a side view of the retainer of FIG. 5.

FIG. 8 is a side view of the retainer of FIG. 5.

FIG. 9 is a cross-section view of the retainer taken along section 9-9of FIG. 5.

FIG. 10 is a cross-section view of the retainer taken along section10-10 of FIG. 5.

FIG. 11 is a cross-section view of the retainer taken along section11-11 of FIG. 5 and illustrates an optional wall or stop member thatextends into the path of the one or more slots in the region of themounting wing.

FIG. 12 is a bottom plan view of the retainer of FIG. 5 and illustratesthat the distance between the side mounting wings varies in the regionof the retainer.

FIG. 13 is a rear side view of the retainer of FIG. 5.

FIG. 14 is a perspective view of an exemplary connector fitting having aspin nut and of a catheter hub with which the securement device of FIG.1 can be used.

FIG. 15 is a perspective view of the connector fitting of FIG. 14 withthe spin nut secured in the forward position and secured to the catheterhub.

FIG. 16 is an exploded, perspective view of the connector fittingsecured to the catheter hub of FIG. 15, both aligned with the first andsecond anchor members and the retainer of FIG. 1.

FIG. 17 is an exploded, perspective view of the connector fittingsecured to the catheter hub of FIG. 15, with the catheter hub beinginserted into the retainer of FIG. 1.

FIG. 18 is a perspective view of the catheter hub secured to thesecurement device of FIG. 1 with gauze inserted between a distal portionof the retainer and the skin surface of the neonate.

FIG. 19 is a perspective view of a securement device having splinesdistributed around the inside of the retainer for engaging anddisengaging with a longitudinal extending member of the retained medicalarticle.

FIG. 20 is a front side view of the retainer of FIG. 19.

FIG. 21 is a perspective view of a connector fitting secured to acatheter hub having a longitudinal extending member for engaging withthe splines on the retainer of FIG. 19.

FIG. 22 is an exploded, perspective view of the connector fittingsecured to the catheter hub of FIG. 21, both aligned with the first andsecond anchor members and the retainer of FIG. 19.

FIG. 23 is a perspective view of the catheter hub secured to thesecurement device of FIG. 19 with the longitudinal extending memberengaged with the splines on the inside of the retainer.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The following description and the accompanying figures, which describeand show preferred embodiments, are made to demonstrate several possibleconfigurations that a securement system can take to include variousaspects and features. The illustrated embodiments are shown in use withan exemplary catheter hub. The illustration of the securement system inthis context is not intended to limit the disclosed aspects and featuresto the specified embodiments or to usage only with the illustrated hub.Those of skill in the art will recognize that the disclosed aspects andfeatures are not limited to any particular embodiment of a securementsystem, and securement systems, which include one or more of theinventive aspects and features herein described, can be designed for usewith a variety of medical articles.

To assist in the description of these components of the securementsystem, the following coordinate terms are used (see FIG. 1). A“longitudinal axis” is generally parallel to a portion of the catheterhub or other medical article retained by the securement system, as wellas parallel to the axis of a channel of the retainer, through which themedical article extends. A “lateral axis” is normal to the longitudinalaxis. A “transverse axis” extends normal to both the longitudinal andlateral axes. In addition, as used herein, “the longitudinal direction”refers to a direction substantially parallel to the longitudinal axis;“the lateral direction” refers to a direction substantially parallel tothe lateral axis; and “the transverse direction” refers to a directionsubstantially parallel to the transverse axis. The term “axial” as usedherein refers to the axis of the channel or medical article, andtherefore is substantially synonymous with the term “longitudinal” asused herein. Also, the terms “proximal” and “distal”, which are used todescribe the present securement system, are used consistently with thedescription of the exemplary applications (i.e., the illustrativeexamples of the use applications). Thus, proximal and distal are used inreference to the center of the patient's body. The terms “upper,”“lower,” “top,” “bottom,” “underside,” “upperside” and the like, whichalso are used to describe the present securement system, are used inreference to the illustrated orientation of the embodiment. For example,the term “upperside” is used to describe the portion of the retainerthat is located above a lateral axis that passes through the axis of thechannel. The term “underside” is used to describe the portion of theretainer that is located below a lateral axis that passes through theaxis of the channel. Brief introductions to some of the features, whichare common to the described embodiments of the securement systems, arenow described. In the illustrated embodiment, the arrows on thesecurement device point in the direction toward the insertion site(i.e., in the proximal direction).

Certain embodiments of the securement device have particularapplicability in connection with securing a medical article to aneonate. The medical article may have an elongated body. The elongatedbody cooperates with the securement device to arrest movement of themedical article in longitudinal, lateral, and transverse directions. Thesecurement device includes a body member and first and second mountingwings. An attachment portion (the longitudinal lengths of the attachmentportions are illustrated in FIG. 2 as 212(a), 212(b)) of the bottomsurface of each mounting wing attaches to an anchor member. The anchormembers adhere to the skin of the neonate.

The attachment portions are disposed within the attachment region (seeattachment region 112 in FIG. 1) when the securement device is securedto the neonate. Due to the difference in size between the medicalarticle and the length of the attachment region on the neonate, theattachment portions of the mounting wings are offset in a proximaldirection relative to the entire longitudinal length of the securementdevice.

The securement device permits the attachment portions of the retainerand the insertion site to both fit in the attachment region on theneonate. As illustrated by FIG. 1, at least a portion of the attachmentregion may be located on either side of the insertion site so as toinhibit movement of the medical article relative to the insertion site.The securement device can also be successfully utilized with any medicalpatient, notwithstanding the size or age of the patient. Thus, theillustration and description of the securement device in context of usea neonate is merely exemplary of one possible application of thesecurement device.

In each of the embodiments described below, the body member includes aninverted channel formed therethrough. The inverted channel has alongitudinal access opening located on an underside of the retainer toallow ingress and egress of the medical article. The medical article isinstalled or removed from the underside of the retainer via this accessopening. Such an arrangement allows the medical provider to align atleast a portion of the medical article with the retainer prior to fixingthe retainer to the neonate's skin. In this way, the inverted channelretains a portion of the medical article.

The retainer includes at least one abutment (can be an abutment surface)that cooperates with at least one contact point or surface on themedical article. The one or more abutment extend generally normal to theaxis of the channel and can be, for example, but without limitation, asurface, a wall of a slot, a ridge, a protuberance, or like structures.The abutment cooperates with the one or more contact points or surfacesof the medical article to inhibit longitudinal movement of the medicalarticle through the channel. For example, the abutment could be asurface on the distal end of the retainer that acts against at least aportion of a radially extending member or spin nut of the medicalarticle. In this way, the medical article will be limited in proximalmovement (i.e., movement toward the patient) once the radially extendingmember contacts or abuts against the distal end of the retainer.

The mounting wings are disposed on the underside of the retainer at aposition lower than the access opening and extend in a proximaldirection away from the body member. The mounting wings provide anattachment surface for adhering the body member to the first and secondanchor members. After the medical article is located in the retainerhealthcare personnel attach the first and second anchor members to theneonate's skin. According to an aspect of the invention, the attachmentportions of the mounting wings are disposed within the attachment regionof the neonate.

Depending on the surface profile of the neonate's skin, a portion of theretainer may be elevated away from the neonate's skin and cantileveredrelative to the attachments portions. For example, the attachment regionmay correspond to a dorsal portion of the neonate's hand (see FIG. 1)such that a distal portion of the retainer is suspended over thefingers. A soft or pliable material may be inserted between the distalportion and the neonate's skin to further inhibit rocking of theretainer relative to the attachment region on the neonate. In such anarrangement, a side view of a secured medical article would illustratethe attachment portions of the mounting wings (and the portions of thefirst and second anchor members transversely aligned with the attachmentportions) offset in a proximal and longitudinal direction from the bodymember.

The retainer and first and second anchor members also can have otherconstructions in order to inhibit contact between the skin and theretainer, as well as between the skin and the retained portion of themedical article. For example, the anchor members can be thicker, inwhich case the lower surface of the mounting wings can be located higheron the body member and still maintain a gap between a secured medicalarticle and the patient's skin.

To facilitate a complete understanding of the embodiment, the remainderof the detailed description describes the securement system withreference to the figures, wherein like elements among the embodimentsare referenced with like numerals throughout the following description.

FIG. 1 is a perspective view of a securement device 100 configured inaccordance with a preferred embodiment of the present invention. FIG. 2is a top plan view of the securement device 100 of FIG. 1 showing a bodymember 130 at least partially offset along a longitudinal and distaldirection from an attachment region 112 on the neonate. The attachmentregion 112 corresponds to the desired location for adhering thesecurement device to the neonate's skin. The attachment region 112illustrated in FIG. 1 extends between the neonate's knuckle 114 andthumb 116. If the length of the attachment region 112 is sufficient toreceive the entire retainer 120 and align the longitudinal axis of themedical article with the insertion site 225, the entire retainer 120 maybe directly secured to the neonate's skin. If the attachment region 112has a longitudinal length less than the overall length of the retainer120, has a longitudinal curvature that prevents the entire retainer 120from contacting the skin of the neonate, or if the desired location ofthe insertion site 225 prevents the entire retainer 120 from beingadhered to the neonate's skin, a distal portion of the retainer 120 maybe elevated from the skin of the neonate. In such instances, thehealthcare provider can insert a soft material, for example, cotton orgauze, between the surface of the neonate and the elevated distalportion of the retainer 120 to thereby limit transverse motion orrocking of the retainer 120 upon the skin.

As shown in FIGS. 1 and 2, the illustrated securement device 100comprises three main components: first and second anchor members 110(a),110(b) and a retainer 120. The retainer 120 includes a first mountingwing 210(a) and a second mounting wing 210(b). The retainer 120 furtherincludes a body member 130.

The first and second mounting wings 210(a), 210(b) are disposed belowthe body member 130 and extend in a proximal and longitudinal directionaway from the body member 130 and generally towards an insertion site225. As described below, a portion of each mounting wing 210(a), 210(b)is disposed upon the respective one of the anchor members 110(a),110(b).

As illustrated in FIG. 2, the mounting wings 210(a), 210(b) arepreferably disposed with respect to the body member 130 such that thetip of the medical article does not extend beyond the front or proximaledge of the mounting wings 210 when the medical article is properlyinserted within the retainer 120. The healthcare provider can beinstructed to generally align the medical article tip with the frontedges of the anchor members 110(a), 110(b) before inserting the medicalarticle into the retainer 120.

As most clearly shown in FIG. 2, the first mounting wing 210(a) has alongitudinal length 214(a). The second mounting wing 210(b) has alongitudinal length 214(b). The first mounting wing 210(a) and thesecond mounting wing 210(b) include attachment portions 212(a), 212(b),respectively. The attachment portions 212(a), 212(b) are spaced apartfrom each other in a lateral direction to define an insertion side spacetherebetween. In the embodiment illustrated in FIG. 2, the insertionside space is generally disposed at a position proximal of the bodymember 130. In the illustrated embodiment, the first and second mountingwings 210(a), 210(b) together support the body member 130 at a distalend of the insertion side space. A location along the mounting wing210(a), 210(b) that is generally equidistant from the proximal anddistal ends of the attachment portion 212(a), 212(b) defines alongitudinal midpoint of the attachment portion 212(a), 212(b).

Each attachment portion 212(a), 212(b) is disposed on a bottom surfaceof a mounting wing 210(a), 210(b). The attachment portions 212(a),212(b) preferably align with at least a portion of the attachment region112 on the neonate's skin. Such an arrangement enhances the stability ofthe securement device 100.

The attachment portion 212(a), 212(b) of each mounting wing correspondswith, and attaches to, a top surface of the corresponding anchor member110(a), 110(b). Preferably, the longitudinal lengths of the attachmentportions 212(a), 212(b) of the mounting wings 210(a), 210(b) are lessthan the corresponding longitudinal lengths 214(a), 214(b) of themounting wings 210(a), 210(b).

FIG. 2 illustrates the attachment portion 212(b) as having alongitudinal length that is less than the longitudinal length 214(b) ofthe second mounting wing 210(b). Since the longitudinal length of theattachment portions 212(a), 212(b) is less than the longitudinal lengthof the corresponding mounting wing 210(a), 210(b), a distal portion ofeach mounting wing located below the body member 130 does not contact oradhere to the corresponding anchor member 110(a), 110(b).

FIG. 2 further illustrates the distal most ends of the attachmentportions 212(a), 212(b) being located at the proximal side of the bodymember 130. Depending on, for example, the length of the attachmentregion 112 that is available for adhering the retainer 120 to theneonate, the distal ends of the attachment portions 212(a), 212(b) canbe disposed so as to correspond to the proximal side of the body member130 or, alternately, to correspond to another longitudinal point inbetween the distal and proximal ends of the mounting wings 210(a),210(b).

Each mounting wing 210(a), 210(b) may include a support arm portion thatlinks the attachment portion 212(a), 212(b) of the mounting wing 210(a),210(b) to the portion of the mounting wing 210(a), 210(b) disposed belowthe body member 130 depending on where the distal end point of theattachment portion 212(a), 212(b) is disposed along the mounting wing210(a), 210(b) relative to the proximal side of the body member 130. Forexample, the distal end point of the attachment portion 212(a), 212(b)may overlap with the body member 130, end at the proximal side of thebody member 130, or be spaced from the proximal side of the body member130 in the proximal direction. When spaced from the proximal side of thebody member 130 in the proximal direction, the region of the mountingwing 210(a), 210(b) located between the distal end point of theattachment portion 212(a), 212(b) and the proximal side of the bodymember 130 defines the support arm portion of the mounting wing 210(a),210(b). Accordingly, some embodiments of the mounting wing 210(a),212(b) may not have a support arm portion. In the embodiment illustratedin FIG. 2 and as most clearly shown in FIG. 12, the distal end point ofthe attachment portion 212(a), 212(b) is disposed at the proximal sideof the body member 130. An embodiment of a support arm 502 is shown inFIG. 19.

The longitudinal lengths of the attachment portion 212(a) and theattachment portion 212(b) are illustrated in FIG. 2 as beingco-extensive. However, it may be advantageous for the length of theattachment portion for the second mounting wing 210(b) to be differentthan the length of the attachment portion for the first mounting wing210(a). Such an arrangement may facilitate attaching the retainer 120 toan attachment region 112 on the neonate that is asymmetric across thelongitudinal axis. Accordingly, one mounting wing 210 may include asupport arm portion having a first longitudinal length while the othermounting wing 210 includes a support arm portion with a differentlongitudinal length or no support arm portion at all.

The lateral widths of the attachment portions 212(a), 212(b) may alsovary between left and right mounting wings 210(a), 210(b). Such aconstruction may further enhance the securement device's applicabilityfor use on uneven or asymmetric surfaces of the neonate's skin.

A perimeter edge or surface 235 around the mounting wings 210(a), 210(b)can be contoured to provide additional protection from chaffing orexfoliation caused by the perimeter edge bearing through the anchormember 110 and upon the neonate's skin. As best illustrated in FIGS. 1and 6, the surface 235 around the perimeter of the mounting wings210(a), 210(b) has a full radius with a diameter that exceeds athickness of the mounting wing 210(a), 210(b). With the diameterexceeding the thickness of the mounting wings 210(a), 210(b), the addedprotection provided by the larger diameter does not substantiallyincrease the weight of the securement device 100.

As noted above, the securement device 100 can form a component of acatheterization or securement system that also includes one or moremedical articles, such as catheters, hubs, catheter adapters, fluidsupply lines, or other articles suitable for securement via the anchormembers and retainer. The catheterization system can also include a softmaterial, such as gauze, cotton, or other material suitable forinsertion into any gap that is formed between the body member 130 andthe neonate's skin. For example, inserting a cotton ball into a gapformed between the distal portion of the retainer 120 and the neonate'sskin may provide additional rigidity to the retainer 120. Such aconstruction may be particularly advantageous when a portion of the bodymember 130 is cantilevered from the attachment region 112 and away fromthe neonate's skin.

Anchor Members

FIGS. 3 and 4 illustrate the first anchor member 110(a) and the secondanchor member 110(b), respectively, apart from the rest of thesecurement device 100 shown in FIG. 2. The general structure of eachanchor member 110(a), 110(b) comprises a generally panhandle shape. Incertain embodiments, the longitudinal extent of the anchor member 110equals or exceeds the longitudinal extent of the attachment portion 212of the corresponding mounting wing 210. Although only a single shape ofthe anchor member is illustrated in FIGS. 3 and 4, those of skill in theart will recognize that a variety of shapes can be used.

Each anchor member 110 comprises a laminate structure with an upperwoven layer and a lower adhesive layer. The upper layer can be polyesteror other suitable polymer or textile materials. One particular suitablematerial is woven polyester available commercially under the name“Tricot” from Tyco. In another variation, the upper layer is a plastic,paper or foam layer (for example, closed-cell polyethylene foam).

The lower adhesive layer constitutes a lower surface 160. The lowersurface is a medical-grade adhesive and can be either diaphoretic ornondiaphoretic, depending upon the particular application. While notillustrated, the anchor members 110(a), 110(b) can include suture holesin addition to the adhesive layer to further secure the anchor member tothe neonate's skin.

In other variations, a hydrocolloid adhesive or zinc oxide-basedadhesive is used upon the anchor members 110(a), 110(b) for attachmentto the skin of the neonate. The hydrocolloid or zinc oxide-basedadhesive can be used either alone or in combination with another medicalgrade adhesive (for example, an adhesive available from Avery DennisonCorporation). Hydrocolloid and zinc oxide-based adhesives have less of atendency to excoriate the skin of a patient when removed. This can beparticularly important for neonates whose skin is more sensitive orfragile.

In variations where the upper layer has a foam surface, the uppersurface 170 can be roughened by corona-treating the foam with a lowelectric charge. The roughened or porous upper surface can improve thequality of the adhesive joint (which is described below) between themounting wings 210 and the anchor member 110.

As illustrated in FIG. 3, a removable paper or plastic release liner 180covers the adhesive lower surface 160 before use. The liner 180 resiststearing and desirably is divided into a plurality of pieces to easeattachment of the tape to a patient's skin.

The liner 180 comprises a folded over portion to define a pull tab 190.The pull tab can be utilized to remove the paper or plastic releaseliner 180 from their adhesive lower surface 160 before use. A healthcareprovider uses the pull tab 190 by grasping and pulling on it so that theliner 180 is separated from the lower surface 160. The pull tab 190overcomes any requirement that the healthcare provider pick at a corneredge or other segment of the liner in order to separate the liner fromthe adhesive layer.

In the embodiment illustrated in FIGS. 3 and 4, the pull tab 190 extendsfrom a bottom surface of the anchor member 110(a), 110(b) and along aninner line 195. The pull tab 190 of course can be designed in a varietyof configurations. For example, the pull tab 190 can be located along acenter line of the anchor member 110; or alternatively, the pull tab canbe located along any line of the anchor member 110 in order to ease theapplication of the anchor member onto the neonate's skin at a specificsite. For example, an area of a neonate's skin with an abrupt bend, suchas at a finger joint, can require that the pull tab 190 be alignedtoward one of the lateral ends of the anchor member 110.

The projection of the release liner beyond the anchor member inner edgeprovides an area onto which any adhesive, which is used to attach theretainer to the anchor member, can run while lessening the occurrence ofsuch adhesive contacting the fold. Cracks often occur at the fold andpresence of adhesive in such cracks can create delimitation of therelease liner and incomplete removal of the release liner when peeledaway from the corresponding anchor member 110(a), 110(b).

Retainer

The retainer 120 is further described with reference to FIGS. 5 through13. FIG. 5 is a top plan view of the retainer 120 of FIG. 2 and furtherillustrates the body member 130 as well as the first and second mountingwings 210(a), 210(b). As illustrated in FIG. 5, the first and secondmounting wings 210(a), 210(b) extend from a proximal most side of thebody member 130.

FIG. 6 is a front side view of the retainer 120. As shown in FIGS. 7 and8, the body member 130 portion of the retainer 120 and the attachmentportions 212(a), 212(b) of the mounting wings 210(a), 210(b) are atleast partially offset from each other along the longitudinal axis.

The body member 130 is elongated in the longitudinal direction andcomprises a generally parallelepiped shape. It is advantageous for thelongitudinal dimension of the body member 130 to be sufficiently long toenhance the stability of the retained portion of the medical articlealong its length. The lateral width of the body member 130 is selectedso as to allow the healthcare provider to easily and naturally grip thesecurement device 100.

With reference to FIG. 6, the inner side of the body member 130 facestowards the patient's skin when in use and defines an inverted centralchannel 140. The inverted channel 140 extends on the underside of thebody member 130 in a longitudinal direction for receiving a section ofthe medical article. A location along the longitudinal direction that isgenerally equidistant from the proximal and distal ends of the bodymember 130 defines a longitudinal midpoint of the channel 140.

The channel 140 is capable of receiving a portion or length of themedical article and is generally configured to house, to grip, and tosecure this portion of the medical article. In the illustratedembodiment (see FIGS. 5 through 8), the central channel 140 has agenerally semi-circular cross-sectional shape. An inner surface contourof the central channel 140 suitably is selected depending on thegeometry of the portion of the medical article to be retained. Forexample, in a retainer 120 that is configured to retain a portion of amedical article that has a constant outer diameter, the central channel140 suitably has a constant radius along its length. In contrast, in aretainer 120 configured to retain a portion of a medical article thathas a tapering outer surface, the central channel 140 suitably has atapering inner surface and a radius that varies along the channellength.

Additional embodiments of the central channel 140 of the retainer cancomprise a plurality of different radii and/or tapering regions. Forexample, the channel 140 can have two sections: a first proximal sectionhave a generally uniform cross-sectional size along its length while asecond distal section has a tapering shape along its length. An abutmentwall may form a transition between these two sections of the channel.These sections of the channel 140 can also both be tapered or straight(i.e., have a generally uniform radius along the length of the section)or the distal section can be straight and the proximal section can betapered. In this way, the size and shape of the central channel 140 canbe chosen to match or to approximate the size and shape of the medicalarticle or portion thereof, e.g., the catheter hub, to be retained.

By matching the inner surface contour of the central channel 140 to theouter surface of the secured portion of the medical article, a moreeffective securement may be achieved. In addition or in the alternative,effective securement can also be achieved by the engagement of one ormore abutment surfaces of the retainer with one or more contact surfaceson the medical article. Each abutment surface can cooperate with acontact surface on the medical article to inhibit movement of themedical article relative to the retainer. Exemplary abutment surfacesand contact surfaces are described below with reference to FIGS. 16-18.

Although the central channel 140 can be formed in various shapesdepending upon the desired application (e.g., depending upon a shape ofthe retained portion of the medical article for which the retainer isdesigned to be used), the central channel 140 desirably has a sufficientlength in the longitudinal direction to stabilize the catheter hub, orother medical article, rather than act as a fulcrum for the fitting.That is, the retainer 120 receives a sufficient length of the catheterhub to inhibit movement of the hub in the lateral, longitudinal andtransverse direction (i.e., to inhibit yaw, pitch and axial movement ofthe article).

As shown most clearly in FIGS. 6 and 12, the lower side of the retainer120 includes an access or lower opening 150. In the illustratedembodiment, the lower opening 150 has generally tapering sides along thelongitudinal axis to match generally the shape of the medical article.In other embodiments, the lower opening 150 has generally parallel sideswhile the channel 140 is tapered to match generally the shape of themedical article. The lower opening 150 may include contouring (e.g.,chamfers) along its periphery in order to guide the medical article intothe central channel 140 when inserting the medical article into theretainer 120.

The illustrated retainer 120 further comprises at least one retentionsurface 165(a), 165(b) disposed on a lower side of the inverted channel140. The at least one retention surface 165 supports the medical articleso that the medical article is elevated in the retainer 120 such thatthe retained portion of the medical article (e.g., the retained portionof the catheter hub) is raised from the neonate's skin to lessen oreliminate compression, excoriation, and/or chaffing of the skin. Thus,the retainer 120 lifts and holds the retained portion of the catheterhub up from the patient's skin.

This support can be provided by, for example, an adhesive, a region ofthe inverted channel which provides a degree of snap-fit with theretained medical article, two or more regions of the inverted channelwhich provide a degree of snap-fit with the retained medical article, ora combination of the adhesive and a region of snap-fit. The adhesive canbe located on one or more surfaces of the retainer 120 that contact themedical article. For example, the adhesive could be located on thesurface of the inverted channel or on an abutment.

As shown most clearly in FIGS. 9 through 11, the present embodiment ofthe retainer 120 includes multiple pairs of retention surfaces 165(a),165(b). The corresponding retention surfaces 165(a), 165(b) of each pairlie on opposite sides of the access opening 150 from each other. In thisembodiment, the retention surface 165(a) is a portion of the surfacethat defines the central channel 140 and is located on the lower side ofthe central channel 140. The retention surface 165(a) is located to oneside of the central axis. The other retention surface 165(b) is aportion of the surface that defines the central channel 140 and islocated on the lower side of the central channel 140. The retentionsurface 165(b) is further located to the side of the central axis thatis opposite to the retention surface 165(a). Once the medical article isplaced in the central channel 140, the retention surfaces 165(a), 165(b)each hold a portion of the retained section of the article within thechannel 140. While multiple retention surfaces are illustrated in FIGS.9 through 11, either retention surface 165(a), 165(b) can beindividually employed in variations of the present retainer and stillsupport the medical article within the channel 140.

As shown most clearly in FIG. 11, the retention surfaces 165(a), 165(b)are both located generally at a distance X measured in a transversedirection from the axis of the central channel 140. Distance X is lessthan radius R when measured at the same location along the centralchannel 140 to elevate the retained medical article above the neonate'sskin.

The retention surfaces 165 provide a degree of snap fit between theretainer 120 and the medical article. The degree of snap-fit can beincreased by extending the overall surface of the central channel 140through an arc of greater than 180°. As shown most clearly in FIG. 6,the arc extends for more than 180 degrees in order to more firmlysupport the retained portion of the medical article. In the illustratedembodiment, the walls of the central channel 140 extend through an arcof approximately 270°. The length of such an arc provides a snap-fitsecurement between the central channel 140 on the body member 130 andthe secured portion of the medical article. In this way, the medicalarticle can be placed in position prior to attaching the securementdevice 100 to the patient without concern that the medical article willshift while healthcare personnel is attaching the device 100 to thepatient. Additionally, the releasable engagement provided by snap-fitconnection also permits the retained portion of the medical article tobe readily released from retainer 120.

In the illustrated embodiment, as best seen in FIG. 11, chamferedsurfaces 240(a) are formed on the underside of the body member 130 alongone of the lower edges of the access opening 150. A second set ofchamfered surfaces 240(b) is formed on the underside of the body member130 along the other lower edge of the access opening 150. The portionsof the body member 130 between these chamfered surfaces 240 and theretention surfaces 165 form hips 270. In other words, the hips 270 arethe portion of the body member 130 that is defined by a lower side ofthe central channel 140 (either the retention surfaces 165(a) on oneside of the central axis or the retention surfaces 165(b) on the otherside of the central axis), the chamfered surfaces 240, and the sides ofthe narrow lower opening 150. In one embodiment, the chamfered surfaces240(a) on one side of the central axis are disposed at an oblique angleto the chamber surfaces 240(b) on the other side of the central axis andhelp guide the medical article into the lower opening 150 and thecentral channel 140.

The retainer 120 can include a generally rigid structure (at least incomparison to foam or tape) and is principally defined by the bodymember 130 and the first and second mounting wings 210(a), 210(b). Thebody member 130, however, may be somewhat flexible in nature, due bothin part to its structure and to the material used to form the bodymember 130. Suitably rigid but flexible materials include, for example,but without limitation: plastics, polymers or composites such aspolypropylene, polyethylene, polycarbonate, polyvinylchloride,acrylonitrile butadiene styrene, nylon, olefin, acrylic, polyester, aswell as moldable silicon, thermoplastic urethane, thermoplasticelastomers, thermoset plastics and the like. However, other materialscan be utilized.

The body member 130 and mounting wings 210(a), 210(b) are integrallyformed to comprise a unitary retainer. This can be accomplished in anyof a variety of ways well known to those skilled in the art. Forinstance, the entire retainer 120 can be injection molded in order toreduce fabrication costs. The illustrated retainer 120 is formed byinjection molding using polyethylene or polypropylene material. Theretainer 120, however, can comprise a non-unitary body member 130 andmounting wings 210(a), 210(b). In this manner, the body member 130 andone or both of the mounting wings 210(a), 210(b) is formed separatelyand then coupled together. Additionally, the body member 130 andmounting wings 210(a), 210(b) can have other forms and can have otherorientations relative to one another. The body member 130 also can beclear or transparent to facilitate alignment of the retainer 120 withthe catheter hub or other medical article during insertion of themedical article through the access opening 150.

As illustrated in FIG. 12, each mounting wing 210(a), 210(b) comprises aglue dam 460 around a portion of its periphery on its underside. Theglue dam restricts adhesive flow beyond an inner edge of the respectivemounting wing. The outer edge of each mounting wing 210(a), 210(b) doesnot include the glue dam (as best seen in FIGS. 11 and 12) to allow anyexcess glue or adhesive to seep out from under the mounting wing duringthe manufacturing process in the lateral direction away from an axisthrough the retainer 120.

As is shown in FIG. 2, the body member 130 is attached to the mountingwings 210(a), 210(b) in a region that is distal of the attachmentportions 212(a), 212(b), however, it need not be so. The attachmentportions 212(a), 212(b) may, or may not, overlap with the body member130.

At least a part of the attachment portion 212(a) of the mounting wing210(a) suitably aligns with the attachment region 112 of the skin of theneonate. Similarly, at least a part of the attachment portion 212(b)suitably aligns with the attachment region 112. The body member 130 andmounting wings are desirably secured to the upper surface of the firstand second anchor members 110(a), 110(b) by a solvent bond adhesive,such as cyanoacrylate or other bonding material. One such adhesive isavailable commercially as Part No. 4693 from 3M.

When the anchor members 110 are secured to the skin of the neonate, themedical article is inhibited from moving substantially in either thelateral or transverse directions relative to the neonate. Longitudinalmovement of the medical article is inhibited by engagement between atleast one abutment surface on the retainer 120 and a contact surface ormating surface on the medical article. The abutment surface on theretainer 120 extends generally normal to the axis of the central channel140. The abutment surface can be located at or between the distal andproximal ends of the retainer 120. For example, the abutment surface canbe either the proximal or distal ends of the retainer. Moreover,multiple abutment surfaces on the retainer 120 can be employed with eachabutment surface being the same or a different type of abutment surface.Additionally, the abutment surface can be used to arrest movement in onelongitudinal direction and the shape of the channel can be used toarrest movement in the opposite longitudinal direction. For example, atleast a portion of the channel 140 can have a tapering inner surface andthe retainer can include an abutment surface in the form of the proximalend of the retainer. The tapering shape and abutment surface cooperateto inhibit longitudinal motion in both longitudinal directions. In suchan embodiment, the tapering surface contacts an outer tapering surfaceof the medical article to limit motion in one direction. Likewise, theproximal end of the retainer abuts with a radially extending member onthe medical article to limit motion in the opposite direction.

The retainer 120 thus includes one or more abutment surfaces. In theillustrated embodiment, the retainer includes multiple abutment surfacesthat are formed by one or more slots 220 in the body member 130. In theform of a slot 220, one abutment surface forms one side of the slot andanother abutment surface forms the other side of the slot 220.

To arrest longitudinal motion in the illustrated embodiment, two contactsurfaces in the form of a single radially extending member are employedon the medical article. The radially extending member extends throughthe slot 220 in the retainer 120 to inhibit longitudinal motion of themedical article in both longitudinal directions. The contact between thetwo abutment surfaces on the retainer 120 and their correspondingcontact surfaces on the medical article arrests motion in thelongitudinal direction. Further embodiments of the retainer 120 inhibitrotational movement of the installed medical article. This will bediscussed in greater detail below.

As shown in FIG. 5, the retainer 120 includes pairs of abutment surfaceswith each pair forming one lateral slot 220 (preferably four abutmentsurfaces form at least two slots) that are sized to receive a radiallyextending portion of the catheter (e.g., a push tab 310 that extendsfrom a catheter hub 430). These slots 220 can extend circumferentiallyabout at least a portion of the axis of the central channel 140. Eachslot has a longitudinal length sufficient to accept the radiallyextending member of the retained medical article.

The radially extending portion of the medical article is in the form ofa push tab 310. An embodiment of a push tab 310 is described withreference to FIGS. 14 and 15. In particular, it can be desirable for thelongitudinal length of each slot to be sufficient to receive the pushtab 310 of the medical article; however, each slot 220 can be slightlylarger than the push tab's thickness (as measured in the longitudinaldirection) and a gap can exist between one or both sides of the push tab310 and the corresponding abutment surfaces that define the slot 220into which the push tab 310 has been inserted. In a preferred form, atleast two or three annular slots 220 are disposed within the retainer120. The longitudinal length of each slot 220 can be about fivethousandths of an inch (0.005 inch, 0.127 mm) larger than the radiallyextending member (e.g., the push tab 310). Such an arrangement can bedesirable to minimize longitudinal movement of the retained portion(e.g., the tab 310 in FIG. 15) of the medical article. Accordingly, asmall gap can exist between any abutment surface and a correspondingcontact surface before the medical article is shifted relative to theretainer 120. Once shifted, however, further longitudinal movement isprevented by the interference between the contact surface and theabutment surface.

Those of skill in the art will recognize that each slot 220 need nothave identical radial extent. The radial extent of each slot 220 neednot be uniform about the axis of the central channel 140.

The inner edges of each slot 220 can be chamfered so as to ease theinsertion of a radially extending member into any slot 220. By havingthe edges of each slot chamfered, it becomes possible to move a radiallyextending member 310 into a slot 220 even if the initial alignmentbetween the center of the slot and the center of the radially extendingmember is not exact. The use of chamfered edges on the slots 220, aswell as the presence of slots located at multiple longitudinal positionsalong the length of the central channel 140, allows for a medicalarticle to be placed into the central channel of the retainer 120 withonly coarse alignment with the axis of the central channel. The medicalarticle generally moves into the nearest slot 220 as the medical articleis pressed up into the retainer 120 from below (that is, as the retainer120 is pressed over the retained portion of the medical article). Thechamfered surfaces 240(a), 240(b) adjacent to the mounting wings 210(a),210(b) help guide the medical article into the central channel 140. Thealignment process is further facilitated when a portion of the retainer120 is transparent.

As shown most clearly in FIGS. 6, 11, and 13, an upper section of theretainer 120 further comprises a depression 135 which forms a finger padthat a healthcare provider can press down upon. The depression 135encourages the finger to push down on the retainer 120 and discouragesthe healthcare provided from gripping the retainer 120 on its sidesduring application. Such a side grip could squeeze or constrict theretainer 120 and make it harder to slip the retainer 120 over themedical article. By pushing down on the retainer 120, this constrictiveeffect is avoided.

As illustrated in FIGS. 6 and 13, a base surface 230 of the retainer 120can have a concave curved shape when viewed from the front and rearsides. The degree of curvature can be varied depending on the expectedlocation of usage or application of the securement device 100. It willbe appreciated that many common sites for insertion of medical lineswhich require securement will be located on anatomical regionsexhibiting convex curvature, such as a dorsal side of a neonate's hand,a arm, a leg, a contact surface, etc. By providing a concave bottomprofile to the retainer 120, the retainer will rock less once placedupon the neonate via the first and second anchor members 110(a), 110(b).

FIGS. 7 and 8 are side views of the retainer 120 of FIG. 5. Asillustrated in FIGS. 7 and 8, an axis 260 of the central channel 140lies at an angle with respect to the base surfaces 230 of the retainer120. The desired angle between the medical article and the patient iscreated by angling the axis 260 of the central channel 140. This angleis selected in order to align the axis 260 of the channel 140 of theretainer with the desired incident angle with which the medical articleis to contact the skin of the neonate.

A variety of different angles for the central channel 140 can be used,ranging from 0° to 45°, and more preferably from 5° to 25°. Forinstance, for the securement of intravenous catheters, it is desirablefor the angle of incidence of the catheter to the skin of the neonate tobe between about 7° to about 15°. For the securement of arterialcatheters, it is desirable for the angle of incident of the catheter tothe skin of the neonate to be about 12.5°. By angling the axis 260 ofthe channel 140 at the desired angle, which will depend upon theparticular securement application (e.g., securing an arterial catheter,an intravenous catheter, etc.), the proper angle of incidence for acatheter can be maintained.

While not illustrated, the retainer 120 can further comprise ribs. Theribs project away from the outside surface of the channel 140. Such ribsmay be formed by extending portions of the slots 220 of the retainer 120away from the channel 140. The ribs provide additional surfaces for thehealthcare provider to grip the retainer 120.

As shown most clearly in FIGS. 5 and 7 through 10, located adjacent tothe slots 220 are upper sections 250. The thickness of the uppersections 250 in the longitudinal direction can vary in order to maintaina generally constant spring force along the entire length of theretainer 120. In this way, the same amount of force is required tospread the walls of the retainer 120 apart even though in theillustrated embodiment the back end of the retainer 120 spreads more toreceive the larger diameter section of a tapered catheter hub 430. Asillustrated in the cross-section views of FIGS. 9 and 10, thelongitudinal and transverse lengths of the upper sections 250 varybetween one or more of the upper sections.

Although certain features of the retainer 120 can be specificallyconfigured for use with a catheter hub 430, it will be understood bythose of skill in the art that such a retainer 120 can be used withother adaptors or medical lines as well.

As shown in FIGS. 5 through 13, each slot 220 is substantially annularin form. However, as illustrated most clearly in FIG. 11, a stop memberor wall 290 extends into the path of the one or more slots 220 at acircumferential location about the axis of the central channel 140. Acomparison of FIGS. 9 and 10 illustrates that the wall 290 in theillustrated embodiment is located on the second mounting wing 210(b)side of the retainer 120. As shown in FIG. 11, the wall 290 in theillustrated embodiment extends in a lateral direction away from thesecond mounting wing 210(b) and into one or more slots 220. In this way,the wall 290 limits the rotation of the radially extending member andmedical article when the medical article is installed in the retainer120. Thus, in the illustrated embodiment, one or more slots 220 extendcircumferentially about the axis of the central channel 140 for lessthan 360 degrees.

The wall 290 can be located at other locations around the circumferenceof the central channel 140. For example, the wall 290 could extend in alateral direction away from the first mounting wing 210(a) and into oneor more slots 220. In embodiments of the retainer 120 where the wall 290extends into less than all of the slots 220, the healthcare provider canselect whether to restrict the rotation of the medical article. Forexample, the healthcare provider can restrict the rotation of themedical article by inserting a radially extending member of the medicalarticle into a slot 220 that includes the wall 290. Alternatively, thehealthcare provider can install the radially extending member into aslot 220 that does not include the wall 290 to allow unbridled rotationof the medical article. Moreover, more than one wall 290 can be locatedaround the circumference of the one or more slots 220 to further limitthe rotation of the medical article. In still further variations of theretainer, the retainer can omit the wall(s) 290.

Each slot 220 has a lateral width sufficient to receive the radiallyextending member of the medical article. In this way, the retainer 120is designed to grip non-winged catheters regardless of the position ofthe radially extending member. For example, in the illustratedembodiment, a catheter hub 430 can be installed into the retainer 120regardless of rotation of the catheter hub 430 about its axis exceptwhen the catheter hub 430 is rotated such that the radially extendingmember coincides with the wall 290. The slot 220 can initially receivethe radially extending member whether the radially extending member ispointing away from the patient, toward the patient, to either side, orgenerally at any other angle about the axis of the catheter hub 430.However, when the radially extending member is pointing directly to theleft side and the catheter hub 430 enters the access opening 150, theradially extending member contacts the wall 290. As the catheter hub 430is further installed into the retainer 120, the catheter hub 430 isforced to rotate such that the radially extending member is pointingdownward. When the radially extending member is pointing downward, theradially extending member will follow the catheter hub 430 into theretainer 120 as the catheter hub 430 is inserted through the accessopening 150. Once the catheter hub 430 has rotated and is subsequentlyfully installed in the retainer 120, the wall 290 will not allow thecatheter hub 430 and radially extending member to rotate completelyabout the axis of the central channel 140. For example, as the catheteradapter is rotated, the radially extending member of the catheter hub430 slides within the slot 220. However, at some point during therotation of the catheter hub 430, the radially extending member contactsthe wall 290.

In the embodiment illustrated in FIGS. 5 through 13, the wall 290 limitsthe rotation of the radially extending member when the push tap issufficiently rotated in either direction towards the second mountingwing 210(b) side of the retainer 120. In this way, the wall 290prohibits the catheter hub 430 from 360-degree rotation while thecatheter hub 430 is installed in the retainer 120.

When the radially extending member points downward (e.g., toward thepatient) and generally normal to the bottom surfaces of the retainer120, the radially extending member extends through the lower opening150. The hips 270 in the lower opening 150 are spaced sufficiently closeto capture the radially extending member in this position and therebyinhibit longitudinal movement of the catheter hub 430.

FIG. 12 is a bottom plan view of an embodiment of the retainer 120 andillustrates that the distance between the first and second mountingwings 210(a), 210(b) varies in the region of the retainer 120. Width W1is measured between the first and second mounting wings 210(a), 210(b)in a lateral direction as shown. Width W2 is measured between the firstand second mounting wings 210(a), 210(b) in a lateral direction asshown.

FIG. 13 is a rear side view of the retainer 120 and further illustratesthe widths W1 and W2 from FIG. 12. The first and second mounting wings210(a), 210(b) are designed so that width W1 is less than the width W2.Width W1 is selected to deter backward insertion of the medical articleinto the retainer 120. For example, the width W1 could be selected to besmaller than a spin nut or the connector end of the catheter hub 430.With W1 less than W2, the potential for the medical article beingincorrectly inserted into the retainer 120 is reduced.

Medical Articles

An exemplary medical article for use with the embodiment of thesecurement device described above will now be described with referenceto FIGS. 14 and 15. The medical article can be a single medical articleor a combination of one or more medical articles. Such medical articlescan be or include, for example, but without limitation, catheters,catheter hubs, catheter adaptors, fluid supply lines, or other similararticles. FIG. 14 is a perspective view of a catheter hub 430 and aconnector fitting 300 with a spin nut 330. The connector fitting 300 isdisposed upon the end of a medical line 360 which can be connected to adrip bag, blood monitor, or other fluid related medical apparatus.

The connector fitting 300 comprises an elongated body 320 which isattached to the end of the medical line 360. The connector fitting 300also comprises a portion that is tapered along at least part of itslongitudinal length so as to allow the end of this region to fit withinthe tapered conical portion of a catheter hub 430. The tapered portion350 of the connector fitting 300 also includes a centrally disposedlumen that communicates with the lumen of the medical line.

FIG. 15 is a perspective view of the connector fitting 300 of FIG. 14with the spin nut 330 secured in the proximal position and secured tothe catheter hub 430. When the connector fitting 300 is inserted intothe catheter hub 430, the lumen of the connector fitting is disposed influid communication with the lumen of the catheter hub 430. Thisprovides fluid communication between the medical line 360 and thepatient.

As seen in FIGS. 14 and 15, the connector fitting 300 has at least twocontact surfaces in the form of one radially extending element 370(a)disposed upon an end of the elongated body 320 of the connector fitting300 opposite the tapered end 350. It may be advantageous for theradially extending element 370(a) to extend completely around thecircumference of the connector fitting 300. Additional contact surfacesin the form of a second radially extending element 370(b) can also bedisposed upon the elongated body 320, as can additional radial elements(not shown). Those of skill in the art will recognize that the radiallyextending element or elements 370(a) need not have any particular shapeor longitudinal thickness. Additionally, the radially extending elementsneed not have the same shape. For instance, the first radially extendingelement 370(a) can have the hexagonal shape illustrated and the secondradially extending element 370(b) can have a circular shape.

A spin nut 330 is disposed upon the connector fitting 300 around theelongated body 320 of the fitting. The spin nut 330 is substantiallycylindrical in form and is able to move upon the connector fitting 300.The spin nut 330 is capable of both rotational motion around the axis ofthe connector fitting and axial motion in both the proximal and distaldirection along the length of the elongated body 320 of the fitting. Thespin nut 330 also includes internal screw threads which are illustratedwith phantom lines in FIGS. 14 and 15.

Still referring to FIGS. 14 and 15, a catheter hub 430 includes a bodythat, in the illustrated embodiment, is configured as a catheter hub 430and has a generally conical shape and tapers from a large radius to asmaller radius along its length. In the illustrated embodiment, thecatheter hub 430 comprises two contact surfaces that together form aradially extending member. The radially extending member can be, forexample, a lateral tab 310 which is disposed at a position along thelength of the body of the hub. The tab 310 can be gripped by thehealthcare provider from the upper side of the retainer 120 in order toimmobilize the catheter hub 430 when unscrewing the spin nut 330 orotherwise disengaging the connector fitting 300 from the catheter hub430. The catheter hub 430 can further include two contact surfaces thattogether form a longitudinal extending member. The longitudinalextending member is further described below in connection with anadditional feature of the securement device 100.

The catheter hub 430 also can include an external screw thread on theoutside of the conical body near the end with the larger radius. Thescrew thread can be used in association with the spin nut 330 of theconnector fitting 300 in order to securely interconnect the connectorfitting 300 and the catheter hub 430.

With reference to FIG. 11, dimensions L1 and L2 illustrate how the wall290 described above prohibits 360-degree rotational movement of thecatheter hub 430 when the catheter hub 430 is installed in the retainer120. Referring to FIGS. 11 and 15, when the catheter hub 430 is fullyinstalled in the retainer 120, the push tap 310 extends in a directionaway from the central axis 340 of the catheter hub 430 and into the slot220. As shown in FIG. 15, a maximum distance from the central axis 340to a distal end of the push tab 310 is distance T. With reference toFIG. 11, to allow the push tab 310 of the catheter hub 430 to rotate inthe region of the mounting wing 210(a), a distance L1 is selected to beequal to or greater than the distance T. The distance L1 is measuredbetween the axis of the central channel 140 and the top surface of thefirst mounting wing 210(a) as shown in FIG. 11. Selecting L1 to begreater than the distance T permits the push tab 310 to rotate past thefirst mounting wing 210(a).

In contrast, to limit rotation of the catheter hub 430 and push tab 310in the region of the second mounting wing 210(b), a distance L2 isselected to be less than the distance T. The distance L2 is measuredbetween the axis of the central channel 140 and the top surface of thewall 290 as shown in FIG. 11. Selecting L2 to be equal to or less thanthe distance T does not permit the push tab 310 to rotate past thesecond mounting wing 210(b).

An advantage of limiting the rotation of the catheter adapter 430 whenit is installed in the retainer 120 can be understood with referenceback to FIG. 14. In FIG. 14, the connector fitting comprises anelongated body 320 which is attached to the end of a medical line. Theother end of the elongated body 320 connects to the catheter adapter orhub 430. The push tab 310 is disposed at a position along the length ofthe body of the hub. The spin nut 330 is disposed around the elongatedbody 320 of the fitting. Internal screw leads within the spin nut 330engage with an external screw thread on the catheter hub 430 in order tosecurely interconnect the connector fitting and the catheter hub 430.

With reference to FIGS. 5 through 13, since the push tab 310 willcontact the wall 290 of the retainer 120 when the spin nut 330 isrotated less than 360 degrees, once the push tab 310 contacts the wall290, the healthcare provider can connect or disconnect the elongatedbody from the catheter adapter 430 without having to also grip the tab310. Once the healthcare provider rotates the fitting in eitherdirection so that the tab 310 contacts the wall 290, the catheter hub430 is effectively immobilized in that direction such that furtherrotation of the catheter hub 430 in that direction is prohibited. Onceimmobilized, the healthcare provider can unscrew the spin nut 330 orotherwise disengage the connector fitting from the catheter hub 430 witha single hand. While the use of two hands may be advantageous in certaincircumstances when operating the spin nut 330, the retainer 120 allowsthe healthcare provider to use a single hand.

Similarly, when connecting or re-connecting the elongated body to thecatheter hub 430, the healthcare provider can initially rotate the pushtab 310, via the spin nut 330, until the push tab 310 contacts the wall290. Once the push tab 310 contacts the wall 290, the catheter hub 430is immobilized which can enhance further connecting of the elongatedbody to the catheter hub 430. In this way, the healthcare provider cancontinue to turn the spin nut 330 until the spin nut 330 is fullyengaged with the catheter hub 430 without having to grip the push tab310 or catheter hub 430.

The retainer 120 can be used with both luer slip and luer lock connectorfittings. The retainer 120 is designed such that even with the push tab310 positioned in the forward most slot 220, the retainer can fit in thespace defined between the push tab 310 and the spin nut 330 with thespin nut 330 fully engaged. The retainer 120 can be further sized toclosely fit within this space to provide redundancy in arrestinglongitudinal movement of the catheter hub 430 relative to the retainer120. Such slots 220 can also be disposed to extend longitudinally toaccommodate radially extending members of greater longitudinal length,such as the splines of a Kipp-style connector. Such splines can befurther distributed around the inside circumference of the invertedchannel 140 to thereby provide a type of indexing as the longitudinalextending member of the retained medical article engages and disengageseach spline while being rotated within the securement device 100 asdescribed below with reference to FIGS. 19 through 23.

Operation

An exemplary process for coupling a medical article with the securementdevice described above will now be described with reference to FIGS. 16through 18. A preferred method of using the embodiment illustrated inFIGS. 1-13 will be described in the context of starting an intravenousline. However, the aspects and features of the operational method andthe use of the present securement device are not limited to thisparticular application.

A healthcare provider begins the procedure by inserting an IV catheterinto a neonate's vein in a known manner and then attaching anintravenous line to the IV catheter though the luer connection. Inparticular, the healthcare provider inserts the tapered or luer end 350of the connector fitting 300 into the catheter hub 430 and then turnsthe spin nut 330 to thread the spin nut 330 over a thread flangedisposed at the distal end of the catheter hub 430. This action drawstogether the two medical article components and releasably interlocksthem. The immediate connection of the IV line to the catheter inhibits aback flow of blood through the catheter. The healthcare provider nowsecures the IV catheter in place on the neonate using the securementdevice 100. In some variations of this method, however, the securementdevice 100 can be first be attached to one or both of the medicalarticle (as well as the possibly to the patient) before the healthcareprovider makes the connection between the two medical articles.

In order to illustrate more clearly the interaction between the retainer120 and the catheter hub 430 in this embodiment, the first and secondanchor members 110(a), 110(b) of the securement device 100 areillustrated as detached from the retainer 120. In accordance with thepreferred embodiment, however, the entire securement device 100 isassembled in accordance with the above-description (e.g., the mountingwings 210 are attached to the anchor members 110) and is sterilizedbefore use.

FIG. 16 is a perspective view of the connector fitting 300 secured tothe catheter hub 430, both aligned with the first and second anchormembers 110(a), 110(b) and the retainer 120. The healthcare provider cansecure a medical line 360 and the medical articles to a patient usingthe above-described securement device 100 or a readily apparentmodification thereof. The healthcare provider aligns the central channel140 of the retainer 120 over the adaptor or catheter hub 430.

FIG. 17 is a perspective view of the connector fitting 300 secured tothe catheter hub 430 with the catheter hub 430 being inserted into theretainer 120. The lower opening 150 in the retainer 120 is pressed overthe catheter hub 430 whereby the catheter hub 430 fitting slides intothe central channel 140 of the body member 130. Depending on thediameter of the catheter hub 430, the retention surface 165 can providea snap-fit connection between the hub and the body member 130. Thecontact surfaces of the catheter hub 430 preferably form one or moreradially extending members 310 (e.g., one or more push tabs or annularcollars), as shown in the illustrated embodiment. The radially extendingmember(s) fits into one (or more) of the lateral slots 220 in theretainer. As can be seen, the tab 310 of the catheter hub 430 lieswithin one of the slots 220 of the retainer 120. In addition, the bodyof the catheter hub 430 generally lies within the central channel 140 ofthe retainer. When guided through the lower opening 150 by thehealthcare provider, the body of the catheter hub 430 will lie withinthe central channel 140 of the retainer 120. The abutment surfaces ofthe slot 220 will inhibit longitudinal migration of the catheter hub 430through the central channel 140 of the retainer 120. Such slots 220 canalso be disposed to extend longitudinally to accommodate radiallyextending members of greater longitudinal length, such as the splines ofa Kipp-style connector as described below with reference to FIGS. 19through 23.

In addition, if used with a connector fitting 300 in which a portion ofthe connector fitting, such as the spin nut 330, has a greater radialsize than the size of the central channel 140 of the retainer 120, thespin nut 330 can act as a contact surface and will inhibit axial motionin one direction through the central channel 140 of the retainer aswell. Using the size of the spin nut 330 or other element having greaterradial size than the size of the channel is not required for effectiveoperation of the systems described herein; however, such a technique maybe an effective form of securement or redundant securement in someapplications.

The combination of the channel shape 140 (both the truncated circularshape and the tapering width), the top portion of the retainer 120, andthe interengagement between the slot(s) 220 and the radially extendingmember(s) 310 on the catheter hub 430 arrest movement of the retainedsection of the medical line in three dimension: longitudinally,laterally and transversely. Further, the wall 290 in the illustratedembodiment prohibits the catheter hub 430 from 360-degree rotation whilethe catheter hub 430 is installed in the retainer 120. The rotationalstop provided by the wall 290 allows the healthcare provider to attachand detach the spin nut 330 (and thus the connector fitting) to andfront the catheter hub 430 without having the remove the catheter hub430 from the retainer. While this feature is preferred in theillustrated application, it is optional and the wall 290 can be omittedfrom the securement device, as noted above.

FIG. 18 is a perspective view of the retainer 120 attached to the anchormembers 110 and securing the catheter hub 430 therein. Once the catheterhub 430 or other medical article enters the access opening 150 of theretainer 120, the first and second anchor members 110(a), 110(b) aresecured to the skin of the neonate such that the attachment portions ofthe left and right mounting wings 210(a), 210(b) are located above theattachment region 112. The central channel 140 of the retainer surroundsan arc length of more than 180 degrees of the medical article. Thisinhibits any transverse or lateral motion of the medical articlerelative to the retainer 120. The catheter hub 430 can be inserted intothe retainer either before or after the fitting connector is attached tothe hub.

The healthcare provider can first remove one portion of the releaseliner 180 from the first anchor member 110(a) by gripping the pull tab190 and pulling the liner 180 away from the lower surface 160 of thefirst anchor member 110(a). This exposes the adhesive layer of the firstanchor member 110(a), which can then be applied to the skin of theneonate near the site where the healthcare provider desires to securethe catheter hub 430 or other medical article. At least parts of theattachment portions 212(a), 212(b) align with at least a portion of theattachment region 112 on the neonate to ensure that the retainer 120 isadequately secured to the neonate. Increasing the amount of the overlapbetween the attachment portions 212(a), 212(b) and the attachment region112 enhances securement to the neonate. As explained above, when thelength of the attachment region 112 on the neonate is less than theoverall length of the retainer 120 or has a longitudinal curvature thatprevents the entire retainer 120 from contacting the skin of theneonate, a distal portion of the retainer 120 may be elevated from thesurface of the neonate. In such instances, a soft material 450, forexample, cotton or gauze can be inserted between the surface of theneonate and the elevated distal portion of the retainer 120 to therebyfurther inhibit transverse motion or rocking of the retainer 120 uponthe skin.

The adhesive layer of the second anchor member 10(b) can be similarlyexposed. The remainder of the release liner 180 for the first and secondanchor members 110(a), 110(b) can then be removed and the anchor members110(a), 110(b) attached to the skin of the neonate. As a variation, therelease liner 180 on one anchor member can be pulled away and the anchormember can be fully attached to the patient before attaching the secondanchor member to the patient.

Additional Embodiments

FIG. 19 is a perspective view of a retainer having splines 1900distributed around the inside of the inverted channel 140 for engagingand disengaging with a longitudinal extending member of the retainedmedical article. The inverted channel 140 of the retainer captures orreceives a longitudinally extending spline 1900 on the medical article.FIG. 20 is a front side view of the retainer from FIG. 19 showing thelongitudinally extending splines 1900.

FIG. 21 is a perspective view of a medical article having a longitudinalextending member 2100 for engaging with the splines 1900 on the retainerof FIG. 19. As illustrated in FIGS. 19 through 23, the splines 1900 canbe distributed around the inside circumference of the inverted channel140 to thereby provide a type of indexing as the longitudinal extendingmember 2100 (see FIG. 21) engages and disengages each spline 1900 as themedical article is rotated within the retainer. FIG. 23 is a perspectiveview of the medical article secured to the retainer of FIG. 19 with thelongitudinal extending member 2100 engaged with the splines 1900 on theinside circumference of the inverted channel 140. Such a constructioncan provide a form of indexing as the retained medical article isrotated within the inverted channel 140.

As understood from the above description of the securement deviceembodiment shown in FIGS. 1-13 and 16-18, the securement device 100attaches to a region on a neonate that can be smaller than the footprintof the securement device since substantial portions of the mounting feet210(a), 210(b) or attachment portions 212(a), 212(b) are offset from thebody member 130 of the retainer 120. In this way, the body member 130grips the medical article at a longitudinal location near to, or outsideof, the attachment region 112 while the offset mounting feet 210(a),210(b) are disposed over the attachment region 112.

The securement device further arrests longitudinal movement of theretained section of the catheter hub 430 by interacting with at leastone and preferably two contact surfaces of the push tab 310, whichconstitutes a radially extending member in the illustrated embodiment.This approach for arresting longitudinal movement can also be used withother types of radially extending members or contacts (e.g., contactsurfaces) on the catheter hub 430 or other medical articles orcomponents thereof.

In other embodiments, the retainer can be configured to fit betweencontacts on a medical article or medical articles. For example, theretainer can be sized to fit between the proximal side of the spin nut330 and the distal side of the push tab 310. In such a case, the endsurfaces of the retainer function as the abutment surfaces and cooperatewith adjacent contacts on the medical article(s). Additionally, theretainer can be configured to not only fit between two contacts on themedical article(s) but also can be configured to receive one or moreradially extending members of the medical article(s).

In a variation of this approach, longitudinal movement can also be fullyarrested (i.e., arrested in both directions along the longitudinal axis)by (1) the interaction of an abutment on the retainer and a distallyfacing contact in combination with (2) the shape of the channel 140. Forexample, in the embodiment described with reference to FIG. 5, thetapering shape of the channel 140, which decreased in size in theproximal direction, inhibited longitudinal movement toward the insertionsite. The interaction between a proximal side wall of the slot 220 andthe distal side of the push tab 310 prevents longitudinal movement inthe distal direction. Thus, some embodiments need only include oneabutment. As noted above, the channel 140 can have a tapering shapealong at least a portion of its length and a step down in diameter alongits length. The tapering shape can arrest longitudinal movement in onedirection and an abutment, which is formed at the diameter step down,can interact with a corresponding contact (e.g., contact surface) on themedical article to arrest longitudinal movement in the oppositedirection.

The various embodiments of securement devices and techniques describedabove thus provide a number of ways to provide safe and releasablesecurement for medical articles to the skin of a patient. In addition,the techniques described may be broadly applied for use with a varietyof medical lines and medical procedures.

Of course, it is to be understood that not necessarily all such objectsor advantages may be achieved in accordance with any particularembodiment of the invention. Thus, for example, those skilled in the artwill recognize that the invention may be embodied or carried out in amanner that achieves or optimizes one advantage or group of advantagesas taught herein without necessarily achieving other objects oradvantages as may be taught or suggested herein. In addition to thevariations described herein, other known equivalents for each featurecan be incorporated by one of ordinary skill in this art to constructanchoring systems in accordance with principles of the presentinvention.

Although this invention has been disclosed in the context of certainpreferred embodiments and examples, it will be understood by thoseskilled in the art that the present invention extends beyond thespecifically disclosed embodiments to other alternative embodimentsand/or uses of the invention and obvious modifications and equivalentsthereof. In particular, while the present retainer has been described inthe context of particularly preferred embodiments, the skilled artisanwill appreciate, in view of the present disclosure, that certainadvantages, features and aspects of the retainer may be realized in avariety of other applications, many of which have been noted above. Forexample, while particularly useful for small-scale applications, such asthe illustrated medical application, the skilled artisan can readilyadopt the principles and advantages described herein to a variety ofother applications, including larger scale devices. Additionally, it iscontemplated that various aspects and features of the inventiondescribed can be practiced separately, combined together, or substitutedfor one another, and that a variety of combination and subcombinationsof the features and aspects can be made and still fall within the scopeof the invention. Thus, it is intended that the scope of the presentinvention herein disclosed should not be limited by the particulardisclosed embodiments described above, but should be determined only bya fair reading of the claims that follow.

1. A securement device for anchoring a medical article to an attachmentregion on a neonate's skin, the securement device comprising: at leastone anchor member having a lower adhesive surface configured to attachto skin of the neonate; and a retainer comprising, a body member havinga channel formed therethrough about a channel axis and terminating at aproximal end of the body member, the channel having a longitudinalaccess opening to allow at least ingress of a portion of the medicalarticle into the channel, the longitudinal access opening extending theentire length of the body member and being disposed on an underside ofthe body member, the channel having a surface that extends through anarc of greater than 180 degrees so as to elevate the portion of themedical article above the skin of the neonate, at least one abutmentextending generally normal to the channel axis so as to inhibitlongitudinal movement of the retained portion of the medical articlerelative to the body member, and at least one mounting wing supportingthe body member and having an attachment portion disposed on a bottomsurface of the at least one mounting wing, the attachment portion beingmounted on the anchor member and directly above the attachment region onthe neonate's skin at least when the at least one anchor member isattached to the skin, the attachment portion being disposed entirely toa proximal side of and beyond the proximal end of the body member, theattachment portion being laterally offset from the body so as to notblock ingress of the portion of the medical article into any portion ofthe channel from a location below the at least one anchor member,wherein a portion of the bottom surface distal to the attachment portionis disposed at least below the body member and outside the attachmentregion on the neonate's skin at least when the at least one anchormember is attached to the skin.
 2. A securement device as in claim 1,wherein the mounting wing includes a support arm that extends from thebody member in a proximal direction and links the body member to theattachment portion.
 3. A securement device as in claim 1, wherein adistal portion of the mounting wing is elevated relative to theattachment portion.
 4. A securement device as in claim 1, wherein the atleast one abutment is located between the proximal end and a distal endof the body member along the axis of the channel.
 5. A securement deviceas in claim 1, wherein the at least one mounting wing supports at leasta portion of the body member at a position elevated relative to at leasta portion of the attachment portion.
 6. A securement device as in claim1, wherein a substantial portion of the at least one mounting wingextends from the body member in a proximal direction.
 7. A securementdevice as in claim 1, wherein the channel has a shape generallycorresponding to a frustoconical shape of a catheter hub, and a distancebetween a proximal end of the at least one each mounting wing and the atleast one abutment substantially equals a distance between a proximalend of the catheter hub and a radially extending member on the catheterhub.
 8. A securement device as in claim 1, wherein the channel has atapering shape.
 9. A securement device as in claim 1, wherein theretainer comprises another abutment disposed such that the abutments atleast substantially oppose each other.
 10. A securement device as inclaim 1, wherein the channel axis is aligned with the skin of thepatient at an angle of approximately 7 degrees when the at least oneanchor member is attached to the skin.
 11. A securement device as inclaim 1, wherein the channel axis is aligned with the skin of thepatient at an angle of approximately 12.5 degrees when the at least oneanchor member is attached to the skin.
 12. A securement device foranchoring a medical article to a patient's skin, the securement devicecomprising: an anchor member; and a retainer comprising a body memberincluding a channel formed therethrough, the channel retaining a portionof the medical article and having a longitudinal access opening disposedon an underside of the body member to allow ingress of the medicalarticle into the channel, at least one abutment extending generallynormal to an axis of the channel to inhibit longitudinal movement of themedical article, and at least one mounting wing supporting the body andhaving an attachment portion mounted to the anchor member, theattachment portion being configured to contact the anchor memberdirectly above the patient's skin, an overall longitudinal length of theat least one mounting wing exceeding the longitudinal length of theattachment portion so that at least a portion of the mounting wingfacing the patient's skin does not contact the patient's skin and doesnot contact the anchor member, an overall lateral width of the at leastone mounting wing being less than a lateral distance from the axis to anouter extremity of the retainer so as to not block ingress of themedical article into the channel from a location below the retainer. 13.A securement device as in claim 12, wherein the mounting wing extendsproximally from the body member from a location on the body member nearthe access opening.
 14. A securement device as in claim 12, wherein theattachment portion of the mounting wing is disposed entirely to one sideof and beyond a proximal end of the body member.
 15. A securement deviceas in claim 12, wherein the at least one mounting wing includes asupport arm that extends from the body member in a proximal directionand links the body member to the attachment portion.
 16. A securementdevice as in claim 12, wherein a distal portion of the at least onemounting wing is elevated relative to the attachment portion.
 17. Asecurement device as in claim 12, wherein the at least one abutment islocated between a proximal end and a distal end of the body member alongthe axis of the channel.
 18. A securement device as in claim 12, whereinthe at least one mounting wing supports at least a portion of the bodymember at a position elevated relative to at least a portion of theattachment portion.
 19. A securement device as in claim 12, wherein asubstantial portion of the at least one mounting wing extends from thebody member in a proximal direction.
 20. A securement device as in claim12, wherein the channel has a shape generally corresponding to afrustoconical shape of a catheter hub, and a distance between a proximalend of the at least one mounting wing and the at least one abutmentsubstantially equals a distance between a proximal end of the catheterhub and a radially extending member on the catheter hub.
 21. Asecurement device as in claim 12, wherein the channel has a taperingshape.
 22. A securement device as in claim 12, wherein the retainercomprises another abutment disposed such that the abutments at leastsubstantially oppose each other.
 23. A securement device as in claim 12,wherein the channel axis is aligned with the skin of the patient at anangle of approximately 7 degrees when the anchor member is attached tothe skin.
 24. A securement device as in claim 12, wherein the channelaxis is aligned with the skin of the patient at an angle ofapproximately 12.5 degrees when the anchor member is attached to theskin.